An experimental study has been carried out on the dynamical process taking place in the secondary plasma generated by a Q-switched Nd:YAG laser (80 mJ, 8 ns) on a copper target at reduced pressure. Accurate dynamical characterization of the cross-sectional view of the plasma has been made possible by the unique combination of a plasma confinement configuration and the time-resolved measurement technique. In addition to reaffirming the role of the blast-wave mechanism in the generation of secondary plasma, an analysis of the time-resolved spatial distributions of emission intensities and the time-resolved spatial distributions of temperature was made. As a result, the occurrence of two-stage emission processes, the “shock excitation stage” and “cooling stage,” has been proved. For instance, at 2 Torr it is shown that the emission process is initiated by a brief shock excitation process (∼ 1 μs) and followed by a longer cooling process (∼ 3 μs). The experimental results concerning the characteristics of the plasma can be well understood by considering the two-stage processes.

Hydrogen emission has been studied in laser plasma by focusing a Nd-YAG laser (1,064 nm, 50 mJ, 8 ns) on various types of samples, such as copper plate, zinc plate and glass plate. Several parameters influencing the emission were varied, such as the type of gas (air, nitrogen and helium), gas pressures (ranging from 2 up to 760 Torr) and laser power density. It was found that H emission with a narrow spectral width occurs with high efficiency when the laser plasma is produced in the low-pressure region. It was also confirmed that the conventional well-known laser-induced breakdown spectroscopy (LIBS), which usually carried out at atmospheric air pressure, cannot be applied for the analysis of hydrogen as impurity. This specific characteristic of the pressure dependence of hydrogen is interpreted based on our shock wave model, taking account of the fact that the hydrogen mass is extremely light compared to that of the host elements.

Global pollution from toxic metal waste has resulted in increased research on toxic metal adsorption. A cellulose acetate–polyurethane (CA–PU) film adsorbent was successfully prepared in this research. The cellulose acetate–polyurethane film adsorbent was prepared with a polycondensation reaction between cellulose acetate and methylene diphenyl diisocyanate. The CA–PU bond formation was confirmed by functional group analysis obtained from Fourier transform infrared (FTIR) spectroscopy. The obtained film was characterized for improved tensile and thermal properties with the addition of methylene diphenyl diisocyanate (MDI). The adsorption ability of the obtained film was evaluated with laser-induced breakdown spectroscopy (LIBS). The best film adsorbent from the LIBS was selected and studied for adsorption isotherm. The FTIR analysis confirmed the formation of the CA–PU bond from the polycondensation between cellulose acetate and the methylene diphenyl diisocyanate. The result showed that the addition of methylene diphenyl diisocyanate (MDI) resulted in the urethane network’s growth. The characterization result showed an improvement in the morphology, thermal stability, and tensile strength of the film. The LIBS studies showed improvement in the adsorption of Pb2+ with CA–PU compared with the neat CA. The isotherm studies revealed that Pb2+ adsorption by cellulose acetate–polyurethane film adsorbent was heterogeneously dependent on the Freundlich isotherm model (R2 = 0.97044). Overall, the polycondensation method proposed by this study enhanced the Pb2+ removal, and was comparable to those reported in previous studies.

A crucial safety measure to be strictly observed in the operation of heavy-water nuclear power plants is the mandatory regular inspection of the concentration of deuterium penetrated into the zircaloy fuel vessels. The existing standard method requires a tedious, destructive, and costly sample preparation process involving the removal of the remaining fuel in the vessel and melting away part of the zircaloy pipe. An alternative method of orthogonal dual-pulse laser-induced breakdown spectrometry (LIBS) is proposed by employing flowing atmospheric helium gas without the use of a sample chamber. The special setup of ps and ns laser systems, operated for the separate ablation of the sample target and the generation of helium gas plasma, respectively, with properly controlled relative timing, has succeeded in producing the desired sharp D I 656.10 nm emission line with effective suppression of the interfering H I 656.28 nm emission by operating the ps ablation laser at very low output energy of 26 mJ and 1 μs ahead of the helium plasma generation. Under this optimal experimental condition, a linear calibration line is attained with practically zero intercept and a 20 μg/g detection limit for D analysis of zircaloy sample while creating a crater only 10 μm in diameter. Therefore, this method promises its potential application for the practical, in situ, and virtually nondestructive quantitative microarea analysis of D, thereby supporting the more-efficient operation and maintenance of heavy-water nuclear power plants. Furthermore, it will also meet the anticipated needs of future nuclear fusion power plants, as well as other important fields of application in the foreseeable future.